FDA UDI In Commercial Distribution 🇺🇸 United States

Profemur

DI: M684PPW383061 · Model: PPW38306 · Microport Orthopedics Inc.
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Profemur
Primary DI
M684PPW383061
Version / Model
PPW38306
Catalog Number
PPW38306
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8e2cef32-b2b9-49db-9621-e6c98eac10eb

Device Description

PROFEMUR 135mm Straight/ Fully Coated/ Plasma Sprayed Size 15.0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
MAY Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish
LWH Counter, Sponge, Surgical

GMDN Terms

Code Name
55833 Press-fit hip femur prosthesis, modular

Identifiers

Type ID
Direct Marking PPW38306
Primary M684PPW383061

Customer Contacts

Device Sizes

Type Value Unit Text
Length 135 Millimeter